rs281875266, F11

N. diseases: 2
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Hereditary Factor XI Deficiency
CUI: C0015523
Disease: Hereditary Factor XI Deficiency
119 1.000 0.080 4 186284163 missense variant G/A;T snv 1.6E-05 0.700 1.000 20 1989 2015
Coagulation factor deficiency syndrome
2 1.000 0.080 4 186284163 missense variant G/A;T snv 1.6E-05 0.700 1.000 1 2019 2019